JPH0499201A - Stainless steel powder for sintering - Google Patents
Stainless steel powder for sinteringInfo
- Publication number
- JPH0499201A JPH0499201A JP2213004A JP21300490A JPH0499201A JP H0499201 A JPH0499201 A JP H0499201A JP 2213004 A JP2213004 A JP 2213004A JP 21300490 A JP21300490 A JP 21300490A JP H0499201 A JPH0499201 A JP H0499201A
- Authority
- JP
- Japan
- Prior art keywords
- powder
- content
- stainless steel
- sintering
- steel powder
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
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- Powder Metallurgy (AREA)
Abstract
Description
【発明の詳細な説明】
〔産業上の利用分野〕
本発明は、ステンレス粉末の射出成形による焼結晶の製
造に係わり、特にステンレス粉末に関す〔従来の技術〕
従来、金属粉末に有機バインダーを配合し混練し、これ
を射出成形し、得られた成形体を脱脂した後焼結する方
法はよく知られている。ここでの脱脂とは、バインダー
を除去する工程であって、熱処理によって行われるのが
一般的である。さらに雰囲気は大きく次の2i!lりに
分けることができる。[Detailed Description of the Invention] [Industrial Application Field] The present invention relates to the production of sintered crystals by injection molding of stainless steel powder, and particularly relates to stainless steel powder [Prior Art] Conventionally, organic binders have been blended with metal powder. A well-known method is to knead the mixture, injection mold it, degrease the resulting molded product, and then sinter it. Degreasing here is a process of removing the binder, and is generally performed by heat treatment. The atmosphere is even bigger next 2i! It can be divided into several parts.
ィ)酸化雰囲気 (Air etc)口)非酸化雰囲
気CNtAr etc)イ)においては、バインダー
を除去するために、バインダーが熱分解あるいは燃焼す
るまでの熱処理温度を上げねばならず、そのためにバイ
ンダーが抜けた後の脱脂体中の粉末は大きく酸化される
。b) Oxidizing atmosphere (Air etc)) Non-oxidizing atmosphere CNtAr etc) In b) In order to remove the binder, it is necessary to raise the heat treatment temperature until the binder thermally decomposes or burns, which causes the binder to come off. After degreasing, the powder in the degreased body is largely oxidized.
焼結時に、C+〇−COの反応においてOを取り除こう
としてもOに見合う分のCが不足しているため、Cによ
って還元されないOが焼結時に残る。脱脂時にバインダ
ーを残す方法も考えられるが、熱分解の途中で脱脂を終
わらせるという方法のため、そのコントロールは非常に
難しい。したがって、焼結体中に還元されない0が残り
、焼結体組織中に介在物、ピンホールを生じさせ機械的
強度が低(なったり、研磨面の光沢が減する等の問題が
あった。At the time of sintering, even if an attempt is made to remove O in the reaction of C+〇-CO, there is insufficient C to cover the amount of O, so O that is not reduced by C remains during sintering. One possibility is to leave the binder behind during degreasing, but it is extremely difficult to control this because the degreasing ends during thermal decomposition. Therefore, unreduced zero remains in the sintered body, causing inclusions and pinholes in the structure of the sintered body, resulting in problems such as low mechanical strength and reduced gloss on the polished surface.
また、口)の雰囲気では、バインダーが熱分解によって
抜けた後の脱脂体中の粉末はほとんど酸化されない。し
かし、バインダーを完全に取り除くことは不可能である
ため、還元に必要以上なCが脱脂体中に残る。したがっ
て、得られた焼結体中にもC量が多く、耐食性を落とし
たり、機械的特性を減する等の問題があった。In addition, in the atmosphere of (1), the powder in the degreased body after the binder is removed by thermal decomposition is hardly oxidized. However, since it is impossible to completely remove the binder, more C than necessary for reduction remains in the degreased body. Therefore, the obtained sintered body also contains a large amount of C, which causes problems such as deterioration of corrosion resistance and mechanical properties.
本発明は、このような課題を解決するためになされたも
のであり、その要旨は非酸化雰囲気で脱脂処理を行い、
その脱脂体中に残留するバインダー中のCを酸化還元反
応により除去するために、残留するCの量に見合うだけ
のOを含む焼結用のステンレス粉末を作製するところで
ある。The present invention was made to solve these problems, and its gist is to perform degreasing treatment in a non-oxidizing atmosphere,
In order to remove C in the binder remaining in the degreased body by redox reaction, stainless steel powder for sintering containing O in an amount corresponding to the amount of remaining C is prepared.
本発明においては、金属粉末の成形体を焼結した時に、
粉末中に含まれるOがC+O−C○の反応を起こし、ガ
スとなって金属粉末より除去される。即ち、脱脂体中に
含有されるCと粉末中に積極的に含有させたOとが互い
に反応して除去される。In the present invention, when a molded body of metal powder is sintered,
O contained in the powder causes a reaction of C+O-C◯, becomes a gas, and is removed from the metal powder. That is, the C contained in the degreased body and the O actively contained in the powder react with each other and are removed.
尚、本発明において粉末中に含有させるべきOの量は、
射出成形体を脱脂した段階の脱脂体に含有されるCの量
によって定まることになる。さらに、このCの量は脱脂
条件によって決まる。したがって、C量を分析して予め
求めておき、その分析値に基づいて必要な0量を計算に
より求めて粉末中に含有させればよい。In addition, in the present invention, the amount of O that should be contained in the powder is
It is determined by the amount of C contained in the degreased injection molded article. Furthermore, the amount of C is determined by the degreasing conditions. Therefore, it is sufficient to analyze and determine the amount of C in advance, calculate the required amount based on the analysis value, and include it in the powder.
上記のように本発明はc+o−coの反応を利用して脱
脂体中のCを除くために、粉末を熱処理によって強制的
に酸化させ、粉末中に○を含有させるところを特徴とし
ている。かかるに本発明によれば、焼結の際に粉末の表
面及び内部に含まれるCが除去されて焼結密度が向上す
るとともに、介在物、ピンホールが著しく少なくなって
U織が良好となり、耐食性、研磨外観の優れた焼結部品
を得ることができる。As described above, the present invention is characterized in that the powder is forcibly oxidized by heat treatment to incorporate O into the powder in order to remove C from the degreased body using the c+o-co reaction. Therefore, according to the present invention, C contained on the surface and inside of the powder is removed during sintering, improving the sintered density, and the number of inclusions and pinholes is significantly reduced, resulting in a good U-weave. Sintered parts with excellent corrosion resistance and polished appearance can be obtained.
次に本発明の特徴をより明確にすべく、以下にその実施
例を詳述する。Next, in order to clarify the characteristics of the present invention, examples thereof will be described in detail below.
実施例−1
平均粒径が10μで酸素量が0.54wt%の水アトマ
イズ法で製造された5US−316粉末を大気炉を使用
し、300℃、2Hで加熱を行った。その後、分析を行
った結果酸素量は0.97wt%であった。Example 1 5US-316 powder produced by water atomization with an average particle diameter of 10 μm and an oxygen content of 0.54 wt% was heated at 300° C. for 2 hours using an atmospheric furnace. Thereafter, analysis revealed that the oxygen content was 0.97 wt%.
この粉末100重量部に対して、ポリスチレンを主成分
とするバインダー11.5重量部を添加し、混線を行っ
た。しかる後、これを射出成形機により7 x 7 x
30mのキャビィティをもつ金型内に温度165℃で成
形し、試験片の成形体を得た。得られた成形体を脱脂炉
で処理することにより、添加したバインダーを熱分解し
た。この操作により添加したバインダーのうち重量で9
5,5%のバインダーが安定的に除去された。この時点
でC量は0.61wt%であった。次に得られた脱脂体
を1150℃までは真空雰囲気でさらに水素を導入して
、最高1320℃にて8時間焼結することにより、焼結
晶が得られた。To 100 parts by weight of this powder, 11.5 parts by weight of a binder containing polystyrene as a main component was added to perform crosstalk. After that, it was molded into 7 x 7 x by injection molding machine.
It was molded at a temperature of 165° C. in a mold having a cavity of 30 m to obtain a molded body of a test piece. The added binder was thermally decomposed by treating the obtained molded body in a debinding furnace. Of the binder added by this operation, 9
5.5% of the binder was stably removed. At this point, the amount of C was 0.61 wt%. Next, hydrogen was further introduced into the obtained degreased body in a vacuum atmosphere up to 1150°C, and sintered crystals were obtained by sintering at a maximum temperature of 1320°C for 8 hours.
その焼結晶の炭素を分析した結果、第1表に示すように
O,0111℃%と低く、また酸素も0.07wt%と
著しく低下していた。As a result of analyzing the carbon content of the fired crystal, as shown in Table 1, O was as low as 0.0111°C%, and oxygen content was significantly reduced to 0.07 wt%.
この焼結晶の耐食性テストを行ったところ、塩水噴霧テ
ストでも、人工汗テストでもさびることはなく良好であ
る。When this baked crystal was tested for corrosion resistance, it showed good results, with no rusting in either the salt spray test or the artificial sweat test.
実施例−2
平均粒径が9.2μで酸素量が0.42vt%の水アト
マイズ法で製造された5LIS−304粉末を大気炉を
使用し、300℃、2Hで加熱処理を行った。Example 2 5LIS-304 powder produced by water atomization with an average particle diameter of 9.2 μm and an oxygen content of 0.42 vt% was heat-treated at 300° C. for 2 hours using an atmospheric furnace.
その後分析を行った結果酸素量は0.89w t%であ
った。この粉末100重量部に対して、アクリルを主成
分とするバインダー10,7重量部を添加した。しかる
後、これを射出成形機により4 X 3 X40口の試
験片金型内に温度170℃で射出成形し、成形体を得た
。得られた脱脂炉で処理することにより、添加したバイ
ンダーのうち重量で96.3%のパインダーが安定的に
除去された。この時点でのC量は0.68wt%であっ
た。次に得られた脱脂体を1120℃までは真空雰囲気
で更に水素を導入して、最高1300℃にて7時間焼結
することにより、焼結密度98%で非常に良好な組織の
焼結品が得られた。Subsequent analysis revealed that the oxygen content was 0.89 wt%. To 100 parts by weight of this powder, 10.7 parts by weight of a binder containing acrylic as a main component was added. Thereafter, this was injection molded into a 4×3×40-mouth test piece mold at a temperature of 170° C. using an injection molding machine to obtain a molded body. By processing in the obtained degreasing furnace, 96.3% by weight of the binder among the added binders was stably removed. The amount of C at this point was 0.68 wt%. Next, the obtained degreased body is further introduced hydrogen in a vacuum atmosphere up to 1120°C and sintered at a maximum of 1300°C for 7 hours, resulting in a sintered product with a sintered density of 98% and a very good structure. was gotten.
その焼結品の炭素を分析した結果、第1表に示すように
0.014wt%と低く、また酸素量も0.059−t
%と著しく低下していた。As a result of analyzing the carbon content of the sintered product, as shown in Table 1, it was as low as 0.014 wt%, and the oxygen content was 0.059-t.
% had decreased significantly.
この焼結品の耐食性テストを行ったところ、塩水噴霧テ
ストでも人工汗テストでもさびることなく良好であった
。When this sintered product was tested for corrosion resistance, it showed good results without rusting in both the salt spray test and the artificial sweat test.
上記の実施例1.2と比較例1〜3を示す第1表の通り
、かかるに本発明によれば、焼結の際に粉末の表面及び
内部に含まれるCが除去されて焼結密度が向上するとと
もに、介在物、ピンホールが著しくなって&llr&が
良好となり、耐食性、研磨外観の優れた焼結部品を得る
ことができるなど、多くの効果を示すものである。As shown in Table 1 showing Example 1.2 and Comparative Examples 1 to 3 above, according to the present invention, carbon contained on the surface and inside of the powder is removed during sintering, resulting in a sintered density It exhibits many effects, such as improved hardness, significant inclusions and pinholes, and good &llr& properties, making it possible to obtain sintered parts with excellent corrosion resistance and polished appearance.
以上 出願人 セイコー電子部品株式会社 代理人 弁理士 林 敬 之 助that's all Applicant: Seiko Electronic Components Co., Ltd. Agent: Patent Attorney Takayoshi Hayashi
Claims (2)
を行い、バインダーを脱脂した後、焼結を行う焼結体の
製造方法の出発材料となる焼結用ステンレス粉末におい
て、脱脂した後に残留した後に残留する炭素を、焼結時
にC+O→COの反応により除去するために、反応に見
合う分だけの酸素を含む焼結用ステンレス粉末。(1) In the stainless steel powder for sintering, which is the starting material for the method of manufacturing a sintered body in which stainless steel powder is mixed with a binder, injection molded, the binder is degreased, and then sintered, the remaining after degreasing Stainless steel powder for sintering that contains oxygen in an amount commensurate with the reaction in order to remove residual carbon through the C+O→CO reaction during sintering.
量が0.8wt%〜1.0wt%であることを特徴とす
る焼結用ステンレス粉末。(2) The stainless steel powder for sintering according to claim 1, wherein the amount of oxygen present in the powder is 0.8 wt% to 1.0 wt%.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2213004A JPH0499201A (en) | 1990-08-09 | 1990-08-09 | Stainless steel powder for sintering |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2213004A JPH0499201A (en) | 1990-08-09 | 1990-08-09 | Stainless steel powder for sintering |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0499201A true JPH0499201A (en) | 1992-03-31 |
Family
ID=16631895
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2213004A Pending JPH0499201A (en) | 1990-08-09 | 1990-08-09 | Stainless steel powder for sintering |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0499201A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007084474A (en) * | 2005-09-21 | 2007-04-05 | Kowa Co | Ophthalmic composition |
-
1990
- 1990-08-09 JP JP2213004A patent/JPH0499201A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2007084474A (en) * | 2005-09-21 | 2007-04-05 | Kowa Co | Ophthalmic composition |
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